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Results: 21 to 40 of 45

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hypokalemic and Hyperkalemic Periodic Paralysis Disorders (NGS Panel and Copy Number Analysis)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
127
  • C Sequence analysis of the entire coding region

Neuromuscular Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
13862
  • C Sequence analysis of the entire coding region

Myastenia Syndrome Panel, Congenital

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
2915
  • C Sequence analysis of the entire coding region

Comprehensive Metabolism NGS Panel

Fulgent Genetics
United States
602355
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Childhood Epilepsy NGS Panel

Fulgent Genetics
United States
354209
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Paramyotonia Congenita (SCN4A Single Gene Test)

Fulgent Genetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Myopathy NGS Panel

Fulgent Genetics
United States
18661
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypokalemic and Hyperkalemic Periodic Paralysis NGS Panel

Fulgent Genetics
United States
145
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nondystrophic Myotonia NGS Panel

Fulgent Genetics
United States
3510
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperkalemic Periodic Paralysis: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Metabolic Myopathy and Rhabdomyolysis

Asper Biogene Asper Biogene LLC
Estonia
6344
  • C Sequence analysis of the entire coding region

PERIODIC PARALYSIS, HYPERKALEMIC

Laboratorio de Genetica Clinica SL
Spain
11
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Neuromuscular Disorders NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
233144
  • C Sequence analysis of the entire coding region

Hyperkalemic Periodic Paralysis Type 2 , Sequencing SCN4A Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Epilepsy Comprehensive NGS Panel

Fulgent Genetics
United States
729398
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Periodic paralysis Panel

CeGaT GmbH
Germany
45
  • C Sequence analysis of the entire coding region

Bartter Syndrome incl. differential diagnosis Panel

CeGaT GmbH
Germany
106
  • C Sequence analysis of the entire coding region

Single gene testing SCN4A

CeGaT GmbH
Germany
51
  • C Sequence analysis of the entire coding region

SCN4A Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
51
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

SCN4A Single Gene

Fulgent Genetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 45

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.